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砷对小鼠成神经瘤细胞N2a的毒性作用 被引量:2

NaAsO2 Induced Neurotoxicity in Mouse Neuroblastoma Cells N2a
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摘要 目的:观察亚砷酸钠对小鼠成神经瘤细胞系N2a细胞的毒性作用。方法:将不同浓度亚砷酸钠对小鼠成神经瘤细胞N2a进行染毒,采用细胞毒性试验(MTS)法观察NaAsO2对N2a细胞的毒性作用,Hoechst33258荧光染色观察凋亡细胞的形态,采用AnnexinV-FITC/PI双重染色的流式细胞检测细胞凋亡率,Caspase-3试剂盒检测Caspase-3酶活性。结果:不同浓度的NaAsO2(10,20,30,40和50μmol/L)作用于N2a细胞,24h后均引起了细胞明显的形态学变化,促进细胞凋亡率,且浓度越大,凋亡效果越明显。结论:NaAsO2对N2a细胞能产生神经毒性,导致细胞凋亡。 Objective: To investigate the toxic effects and possible mechanisms of NaAsO2 in the mouse neuroblasto- ma cell line (N2a). Methods:Cultured N2a cells were exposed to NaAsO2( 10,20,30,40 and 50p, mol/L) for 24h. MTS assay was used to evaluate the cell viability. A flow cytometry assessment with Armexin V-FITC/PI and apoptotic morpholo- gy were used to detect apoptosis induced by NaAsO2. Results:The results showed that NaAsO2 at 24 h substantially altered the morphology and significantly induced apoptosis ( P 〈 0.05 ). Conclusion: An increased concentration of NaAsO2 elevat- ed the apoptotic effect in N2a cells.
出处 《农垦医学》 2012年第6期488-491,共4页 Journal of Nongken Medicine
基金 国家自然科学基金项目(30960338) 新疆生产建设兵团博士基金项目(2011BB019) 新疆生产建设兵团重点领域科技攻关项目(2011BA0158)
关键词 小鼠成神经瘤细胞N2a 细胞凋亡 Arsenite N2a Aportosis
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参考文献2

  • 1Bradley MM, Siperko LM, Porter MD. Colofimetric-solid phase ex- traction method for trace level determination of arsenite in water [ J ]. Talanta,2011,86:64 - 70.
  • 2Menge-orf T, Althausen S, Paschen W. Genes associated with pro- apoptotic and protective mechanisms are affected differently on ex- posure of neuronal cell cultures to arsenite. No indication for endo- plasmic reticulum stress despite activation of grp78 and gadd153 expression[J]. Brain Res Mol Brain Res,2002,104(2):227 - 239.

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